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PERIMETER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113642
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2012
Days to Decision
56 days
Submission Type
Summary

PERIMETER INTERBODY FUSION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K113642
510(k) Type
Traditional
Applicant
MEDTRONIC SOFAMOR DANEK USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/6/2012
Days to Decision
56 days
Submission Type
Summary